TY - JOUR
T1 - Feasibility and Effect of Increasing Clozapine Plasma Levels in Long-Stay Patients with Treatment-Resistant Schizophrenia
AU - Bogers, Jan P. A. M.
AU - Schulte, Peter F. J.
AU - Broekman, Theo G.
AU - de Haan, Lieuwe
N1 - Publisher Copyright: © 2023 Wolters Kluwer Health, Inc.
PY - 2023/3/1
Y1 - 2023/3/1
N2 - Background It is unknown whether increasing the clozapine plasma level to 400, 750, or even 1000 ng/mL is a feasible and effective strategy in patients with treatment-resistant schizophrenia (TRS). We investigated this in long-stay patients with TRS. Methods In long-stay TRS patients, doses of clozapine were increased gradually to reach target plasma levels of 400, 750, or 1000 ng/mL, depending on the clinical response and tolerability. After an effective or tolerated level was reached, positive and negative syndrome scale scores were evaluated after 3 months and 1 year. Results Twenty-eight patients were included. Overall, 54% of the patients, and especially patients 60 years and older, could not achieve one of the clozapine target levels because of adverse effects. Three physically vulnerable patients died, probably not directly related to clozapine use. Although only 21% of patients achieved a more than 20% reduction in total symptoms at the 1-year follow-up, the mean severity of positive symptoms decreased from 18.18 to 15.10 (P < 0.01). The largest decrease in positive symptoms was seen in TRS patients who achieved a plasma level of 750 ng/mL of clozapine. Conclusions Most TRS patients older than 60 years could not tolerate high clozapine levels and so this should not be attempted in older or otherwise physically vulnerable patients. Increasing clozapine levels to approximately 750 ng/mL in middle-aged patients with longstanding TRS may modestly reduce the severity of positive symptoms and improve the response rate.
AB - Background It is unknown whether increasing the clozapine plasma level to 400, 750, or even 1000 ng/mL is a feasible and effective strategy in patients with treatment-resistant schizophrenia (TRS). We investigated this in long-stay patients with TRS. Methods In long-stay TRS patients, doses of clozapine were increased gradually to reach target plasma levels of 400, 750, or 1000 ng/mL, depending on the clinical response and tolerability. After an effective or tolerated level was reached, positive and negative syndrome scale scores were evaluated after 3 months and 1 year. Results Twenty-eight patients were included. Overall, 54% of the patients, and especially patients 60 years and older, could not achieve one of the clozapine target levels because of adverse effects. Three physically vulnerable patients died, probably not directly related to clozapine use. Although only 21% of patients achieved a more than 20% reduction in total symptoms at the 1-year follow-up, the mean severity of positive symptoms decreased from 18.18 to 15.10 (P < 0.01). The largest decrease in positive symptoms was seen in TRS patients who achieved a plasma level of 750 ng/mL of clozapine. Conclusions Most TRS patients older than 60 years could not tolerate high clozapine levels and so this should not be attempted in older or otherwise physically vulnerable patients. Increasing clozapine levels to approximately 750 ng/mL in middle-aged patients with longstanding TRS may modestly reduce the severity of positive symptoms and improve the response rate.
KW - adverse effects
KW - clozapine
KW - high plasma levels
KW - intolerance
KW - positive symptoms
UR - http://www.scopus.com/inward/record.url?scp=85149180636&partnerID=8YFLogxK
U2 - https://doi.org/10.1097/JCP.0000000000001657
DO - https://doi.org/10.1097/JCP.0000000000001657
M3 - Article
C2 - 36825865
SN - 0271-0749
VL - 43
SP - 97
EP - 105
JO - Journal of clinical psychopharmacology
JF - Journal of clinical psychopharmacology
IS - 2
ER -